DPY30 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging Mutations in this gene have

Mutations in this gene have been associated with congenital myasthenic syndrome

Contains 5 C2H2-type zinc fingers

Mutations in this gene cause Charcot-Marie-Tooth disease type 1C (CMT1C) and may be involved in the carcinogenesis of extramammary Paget's disease (EMPD)

particularly on chromosomes Y and 15

It is a component of the tumor necrosis factor (TNF) receptor-I signaling complex

DPY30 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging Mutations in this gene haveThis gene encodes an integral core subunit of the SET1 MLL family of H3K4 methyltransferases. The encoded protein directly controls cell cycle regulators and plays an important role in the proliferation and differentiation of human hematopoietic progenitor cells.